The arrojadite enigma; II, Compositional space, new members, and nomenclature of the group
The arrojadite enigma; II, Compositional space, new members, and nomenclature of the group
American Mineralogist (August 2006) 91 (8-9): 1260-1270
- Canada
- cell dimensions
- chemical composition
- crystal chemistry
- crystal structure
- electron probe data
- formula
- granites
- hydroxyl ion
- ICP mass spectra
- igneous rocks
- laser ablation
- laser methods
- lattice parameters
- mass spectra
- new minerals
- optical properties
- pegmatite
- phosphates
- plutonic rocks
- Raman spectra
- refinement
- single-crystal method
- spectra
- Western Canada
- X-ray diffraction data
- Yukon Territory
- arrojadite
- dickinsonite
- sigismundite
A systematic chemical and structural investigation of arrojadite-group minerals has provided new data allowing us to design a consistent nomenclature scheme, approved by the IMA CNMMN (vote 05-D). The cornerstones of this scheme are: (1) the fundamental structural formula for the arrojadite group is A (sub 2) B (sub 2) Ca Na (sub 2+x) M (sub 13) Al (PO (sub 4) ) (sub 11) (PO (sub 3) OH (sub 1-x) ) W (sub 2) , where A are either large divalent cations (Ba, Sr, Pb) plus vacancy, or monovalent (K, Na) cations, B are either small divalent cations (Fe, Mn, Mg) plus vacancy, or monovalent (Na) cations. (2) The dominant cation at the M sites defines the root-name: Fe (super 2+) , arrojadite; Mn (super 2+) , dickinsonite; Mg (if any), name to be proposed. (3) Two suffixes are added to the root-name according to the dominant cation of the dominant valence state at the A1 and B1 sites (the mono- or divalent nature of the cation used implicitly specifies the dominant occupancy by Na or the dominant vacancy, respectively, at the A (sub 2) and B (sub 2) sites, according to two heterovalent substitutions). (4) A third suffix is added in case the sum of non-(P,Al) cations exceeds 20.5 apfu [which implies that the Na3 site is more than half occupied and the total (OH,F) content is less than 2.5 apfu]. (5) Prefixes may be added to the root-name in the case of dominance of F over OH at the W site or of Fe (super 3+) over Al at the Al site. The compositional range explored is quite large, with either K, Sr, Ba, or Pb as the dominant cation at A1; Na, Fe, or Mn dominant at B1; Na or vacancies dominant at A2 and B2; Na or vacancy at the Na3 site; and F or OH at the W site. Lithium can amount up to 1 Li pfu and is partitioned into the M sites, preferentially M1. As a consequence of this new nomenclature scheme, the mineral name "sigismundite" is abolished and the corresponding composition must be referred to as arrojadite-(BaFe). In addition, arrojadites-dickinsonites from classic localities are identified as arrojadite-(KFe) (Nickel Plate Mine), dickinsonite-(KMnNa) (Branchville), fluorarrojadite-(BaFe) (Sidi-bou-Kricha), and we define the new members arrojadite-(KNa) (Rapid Creek), arrojadite-(PbFe) (Sapucaia), and arrojadite-(SrFe) (Horrsjoberg).